Cargando…

Infection of Two Heterologous Mycoviruses Reduces the Virulence of Valsa mali, a Fungal Agent of Apple Valsa Canker Disease

Mycovirus infection has been widely shown to attenuate the virulence of phytopathogenic fungi. Valsa mali is an agriculturally important fungus that causes Valsa canker disease in apple trees. In this study, two unrelated mycoviruses [Cryphonectria hypovirus 1 (CHV1, genus Hypovirus, and single-stra...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Shian, Dai, Ruoyin, Salaipeth, Lakha, Huang, Lili, Liu, Jie, Andika, Ida Bagus, Sun, Liying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186502/
https://www.ncbi.nlm.nih.gov/pubmed/34113326
http://dx.doi.org/10.3389/fmicb.2021.659210
_version_ 1783704960765001728
author Yang, Shian
Dai, Ruoyin
Salaipeth, Lakha
Huang, Lili
Liu, Jie
Andika, Ida Bagus
Sun, Liying
author_facet Yang, Shian
Dai, Ruoyin
Salaipeth, Lakha
Huang, Lili
Liu, Jie
Andika, Ida Bagus
Sun, Liying
author_sort Yang, Shian
collection PubMed
description Mycovirus infection has been widely shown to attenuate the virulence of phytopathogenic fungi. Valsa mali is an agriculturally important fungus that causes Valsa canker disease in apple trees. In this study, two unrelated mycoviruses [Cryphonectria hypovirus 1 (CHV1, genus Hypovirus, and single-stranded RNA) and Mycoreovirus 1 (MyRV1, genus Mycoreovirus, double-stranded RNA)] that originated from Cryphonectria parasitica (chestnut blight fungus) were singly or doubly introduced into V. mali via protoplast fusion. CHV1 and MyRV1 stably infected V. mali and caused a reduction in fungal vegetative growth and virulence. Co-infection of both viruses further reduced the virulence of V. mali but compromised the stability of CHV1 infection and horizontal transmission through hyphal anastomosis. Infections of MyRV1 and, to a lesser extent, CHV1 up-regulated the transcript expression of RNA silencing-related genes in V. mali. The accumulation of CHV1 (but not MyRV1) was elevated by the knockdown of dcl2, a key gene of the RNA silencing pathway. Similarly, the accumulation of CHV1 and the efficiency of the horizontal transmission of CHV1 during co-infection was restored by the knockdown of dcl2. Thus, CHV1 and MyRV1 are potential biological control agents for apple Valsa canker disease, but co-infection of both viruses has a negative effect on CHV1 infection in V. mali due to the activation of antiviral RNA silencing by MyRV1 infection.
format Online
Article
Text
id pubmed-8186502
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-81865022021-06-09 Infection of Two Heterologous Mycoviruses Reduces the Virulence of Valsa mali, a Fungal Agent of Apple Valsa Canker Disease Yang, Shian Dai, Ruoyin Salaipeth, Lakha Huang, Lili Liu, Jie Andika, Ida Bagus Sun, Liying Front Microbiol Microbiology Mycovirus infection has been widely shown to attenuate the virulence of phytopathogenic fungi. Valsa mali is an agriculturally important fungus that causes Valsa canker disease in apple trees. In this study, two unrelated mycoviruses [Cryphonectria hypovirus 1 (CHV1, genus Hypovirus, and single-stranded RNA) and Mycoreovirus 1 (MyRV1, genus Mycoreovirus, double-stranded RNA)] that originated from Cryphonectria parasitica (chestnut blight fungus) were singly or doubly introduced into V. mali via protoplast fusion. CHV1 and MyRV1 stably infected V. mali and caused a reduction in fungal vegetative growth and virulence. Co-infection of both viruses further reduced the virulence of V. mali but compromised the stability of CHV1 infection and horizontal transmission through hyphal anastomosis. Infections of MyRV1 and, to a lesser extent, CHV1 up-regulated the transcript expression of RNA silencing-related genes in V. mali. The accumulation of CHV1 (but not MyRV1) was elevated by the knockdown of dcl2, a key gene of the RNA silencing pathway. Similarly, the accumulation of CHV1 and the efficiency of the horizontal transmission of CHV1 during co-infection was restored by the knockdown of dcl2. Thus, CHV1 and MyRV1 are potential biological control agents for apple Valsa canker disease, but co-infection of both viruses has a negative effect on CHV1 infection in V. mali due to the activation of antiviral RNA silencing by MyRV1 infection. Frontiers Media S.A. 2021-05-25 /pmc/articles/PMC8186502/ /pubmed/34113326 http://dx.doi.org/10.3389/fmicb.2021.659210 Text en Copyright © 2021 Yang, Dai, Salaipeth, Huang, Liu, Andika and Sun. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Yang, Shian
Dai, Ruoyin
Salaipeth, Lakha
Huang, Lili
Liu, Jie
Andika, Ida Bagus
Sun, Liying
Infection of Two Heterologous Mycoviruses Reduces the Virulence of Valsa mali, a Fungal Agent of Apple Valsa Canker Disease
title Infection of Two Heterologous Mycoviruses Reduces the Virulence of Valsa mali, a Fungal Agent of Apple Valsa Canker Disease
title_full Infection of Two Heterologous Mycoviruses Reduces the Virulence of Valsa mali, a Fungal Agent of Apple Valsa Canker Disease
title_fullStr Infection of Two Heterologous Mycoviruses Reduces the Virulence of Valsa mali, a Fungal Agent of Apple Valsa Canker Disease
title_full_unstemmed Infection of Two Heterologous Mycoviruses Reduces the Virulence of Valsa mali, a Fungal Agent of Apple Valsa Canker Disease
title_short Infection of Two Heterologous Mycoviruses Reduces the Virulence of Valsa mali, a Fungal Agent of Apple Valsa Canker Disease
title_sort infection of two heterologous mycoviruses reduces the virulence of valsa mali, a fungal agent of apple valsa canker disease
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186502/
https://www.ncbi.nlm.nih.gov/pubmed/34113326
http://dx.doi.org/10.3389/fmicb.2021.659210
work_keys_str_mv AT yangshian infectionoftwoheterologousmycovirusesreducesthevirulenceofvalsamaliafungalagentofapplevalsacankerdisease
AT dairuoyin infectionoftwoheterologousmycovirusesreducesthevirulenceofvalsamaliafungalagentofapplevalsacankerdisease
AT salaipethlakha infectionoftwoheterologousmycovirusesreducesthevirulenceofvalsamaliafungalagentofapplevalsacankerdisease
AT huanglili infectionoftwoheterologousmycovirusesreducesthevirulenceofvalsamaliafungalagentofapplevalsacankerdisease
AT liujie infectionoftwoheterologousmycovirusesreducesthevirulenceofvalsamaliafungalagentofapplevalsacankerdisease
AT andikaidabagus infectionoftwoheterologousmycovirusesreducesthevirulenceofvalsamaliafungalagentofapplevalsacankerdisease
AT sunliying infectionoftwoheterologousmycovirusesreducesthevirulenceofvalsamaliafungalagentofapplevalsacankerdisease